Cell Migration Chip (3DCM-chip): a New Tool Toward the Modelling of 3D Cellular Complex Systems.

Breast cancer CAFs Co‐cultures PEG‐fibrinogen cellular invasion

Journal

Advanced healthcare materials
ISSN: 2192-2659
Titre abrégé: Adv Healthc Mater
Pays: Germany
ID NLM: 101581613

Informations de publication

Date de publication:
13 May 2024
Historique:
revised: 24 04 2024
received: 04 01 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 13 5 2024
Statut: aheadofprint

Résumé

3D hydrogel-based cell cultures provide models for studying cell behavior and can efficiently replicate the physiologic environment. Hydrogels can be tailored to mimic mechanical and biochemical properties of specific tissues and allow to produce gel-in-gel models. In this system, microspheres encapsulating cells are embedded in an outer hydrogel matrix, where cells are able to migrate. To enhance the efficiency of such studies, we design a lab-on-a-chip named 3D Cell Migration-chip (3DCM-chip) that offers substantial advantages over traditional methods. 3DCM-chip facilitates the analysis of biochemical and physical stimuli effects on cell migration/invasion in different cell types, including stem, normal and tumor cells. 3DCM-chip provides a smart platform for developing more complex cell co-cultures systems. Herein we investigate the impact of human fibroblasts on MDA-MB 231 breast cancer cells invasiveness. Moreover, how the presence of different cellular lines, including mesenchymal stem cells (hMSCs), normal human dermal fibroblasts (NHDFs), and human umbilical vein endothelial cells (HUVECs), affects the invasive behavior of cancer cells is investigated using 3DCM-chip and producing predictive tumoroid models with a more complex network of interactions between cells and microenvironment. 3DCM-chip moves us closer to creating in vitro systems that can potentially replicate key aspects of the physiological tumor microenvironment. This article is protected by copyright. All rights reserved.

Identifiants

pubmed: 38739022
doi: 10.1002/adhm.202400040
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2400040

Informations de copyright

This article is protected by copyright. All rights reserved.

Auteurs

Silvia Buonvino (S)

Department of Experimental Medicine, University of Rome Tor Vergata, Rome, 00133, Italy.

Davide Di Giuseppe (DD)

Department of Electronic Engineering, University of Rome Tor Vergata, Rome, 00133, Italy.

Joanna Filippi (J)

Department of Electronic Engineering, University of Rome Tor Vergata, Rome, 00133, Italy.

Eugenio Martinelli (E)

Department of Electronic Engineering, University of Rome Tor Vergata, Rome, 00133, Italy.

Dror Seliktar (D)

Department of Biomedical Engineering, Technion Israel Institute of Technology, Haifa, 3200003, Israel.

Sonia Melino (S)

Department of Chemical Science and Technologies, University of Rome "Tor Vergata", via della Ricerca Scientifica, Rome, 00133, Italy.
NAST Center- University of Rome Tor Vergata, Italy.

Classifications MeSH